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Impact of photobiomodulation on pain associated with orthodontic treatment

Impact of photobiomodulation on pain associated with orthodontic treatment with clear aligners or fixed appliances - a retrospective, multicentre study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN16566195
Enrollment
32
Registered
2024-03-01
Start date
2023-10-03
Completion date
Unknown
Last updated
2024-08-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Reduction of pain associated with orthodontic treatment in patients undergoing orthodontic treatment Oral Health

Interventions

Upon starting orthodontic treatment with either clear aligners or fixed appliances, some patients were asked to use the PBM Ortho device and to record their pain level every day for 7 days, and some p

Sponsors

PBM Healing International Limited
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Systemically healthy male and female patients (age 18 - 65), i.e., did not suffer from systemic illness nor require medication during the study period. 2. Permanent dentition, with Little's Irregularity Index (LII) of 2 mm or greater for the upper and lower arch. 3. Orthodontic treatment using clear aligners or fixed appliances via non-extraction therapy. 4. Non-smoker with no use of chewing tobacco. 5. Good oral hygiene. 6. Caries free. 7. No sign of periodontal disease.

Exclusion criteria

Exclusion criteria: 1. Systemic diseases 2. Medication use for the past 6 months; especially use of anti-inflammatory (e.g., NSAIDs) 3. Smoking. 4. Active dental caries. 5. Any periodontal problem including bleeding, tooth mobility, bone loss, attachment loss, deep pockets. 6. Sleep apnea and other airway pathologies 7. Photosensitivity or use of drugs that may cause photosensitivity 8. Use of osteoporosis drugs 9. Epilepsy 10. Patients who had an implanted cardiac device unless the device is known to not be affected by magnetic fields

Design outcomes

Primary

MeasureTime frame
Self-reported pain level for 7 days using a visual analog scale form (0 = no pain, 10 = worst pain imaginable)

Secondary

MeasureTime frame
Any report of adverse events measured using patient records throughout the study

Countries

Japan

Contacts

Public ContactAlan Kwong Hing
dr.al@pbmhealing.com+852 3611 2573

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026